Skip to content

Locking Drill Guide 231200109

by Biomet Orthopedics, Inc.

Ref 231200109

Locking Drill Guide 231200109 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 24 Oct 2026 (Basic UDI-DI B-00880304533554) and listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00880304533554), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00880304533554 Basic UDI-DI 00880304533554UDI-DIDate24 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00880304533554 UDI-DI Date28 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00880304533554 registered 24 Oct 2026 Active
  • FDA GUDID UDI-DI 00880304533554 listed 28 Jul 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00880304533554
  2. Registered EUDAMED B-00880304533554

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Locking Drill Guide
Generic name
Surgical drill guide, reusable
Device name
DVR Crosslock Drill Guide Locking 2.2mm
Model / Ref / Catalog
231200109
Primary DI / UDI-DI
00880304533554
Basic UDI-DI
B-00880304533554
FDA product code
HTW
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
GMDN term
Surgical drill guide, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical drill guide, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)